1. Chapter 20 Carboxylic Acids
Organic Chemistry, 7th Edition L. G. Wade, Jr.
Chapter 20
Carboxylic Acids
Copyright © 2010 Pearson Education, Inc.

2. Deprotonation of Carboxylic Acids
The hydroxide ion deprotonates the acid to form the acid salt.
Adding a mineral acid regenerates the carboxylic acid.
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3. Naming Carboxylic Acid Salts
First name the cation.
Then name the anion by replacing the -ic acid with -ate. C H 3 2 O - K + l
potassium 3-chloropentanoate
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4. Hydrolysis of Fats and Oils
The basic hydrolysis of fat and oils produces soap (this reaction is known as saponification).
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5. Extraction of Carboxylic Acids
A carboxylic acid is more soluble in the organic phase, but its salt is more soluble in the aqueous phase.
Acid–base extractions can move the acid from the ether phase into the aqueous phase and back into the ether phase, leaving impurities behind.
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6. Some Important Acids
Acetic acid is in vinegar and other foods, used industrially as solvent, catalyst, and reagent for synthesis.
Fatty acids from fats and oils.
Benzoic acid in found in drugs and preservatives.
Adipic acid used to make nylon 66.
Phthalic acid used to make polyesters.
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7. IR Bands of Carboxylic Acids
There will be two features in the IR spectrum of a carboxylic acid: the intense carbonyl stretching absorption (1710 cm-1) and the OH absorption (2500–3500 cm-1) .
Conjugation lowers the frequency of the C═O band.
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8. IR Spectroscopy
O—H
C═O
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9. NMR of Carboxylic Acids
Carboxylic acid protons are the most deshielded protons we have encountered, absorbing between d10 and d13.
The protons on the a-carbon atom absorb between d2.0 and d2.5.
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10. NMR Spectroscopy
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11. Fragmentation of Carboxylic Acids
The most common fragmentation is the loss of an alkene through the McLafferty rearrangement.
Another common fragmentation is cleavage of the b-g bond to form an alkyl radical and a resonance-stabilized cation.
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12. Mass Spectrometry
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13. Synthesis Review
Oxidation of primary alcohols and aldehydes with chromic acid.
Cleavage of an alkene with hot KMnO4 produces a carboxylic acid if there is a hydrogen on the double-bonded carbon.
Alkyl benzene oxidized to benzoic acid by hot KMnO4 or hot chromic acid.
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14. Oxidation of Primary Alcohol to Carboxylic Acids
Primary alcohols and aldehydes are commonly oxidized to acids by chromic acid (H2CrO4 formed from Na2Cr2O7 and H2SO4).
Potassium permanganate is occasionally used, but the yields are often lower.
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15. Cleavage of Alkenes Using KMnO4
Warm, concentrated permanganate solutions oxidize the glycols, cleaving the central C═C bond.
Depending on the substitution of the original double bond, ketones or acids may result.
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16. Alkyne Cleavage Using Ozone or KMnO4
With alkynes, either ozonolysis or a vigorous permanganate oxidation cleaves the triple bond to give carboxylic acids.
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17. Side Chain Oxidation of Alkylbenzenes
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18. Conversion of Grignards to Carboxylic Acids
Grignard reagent react with CO2 to produce, after protonation, a carboxylic acid.
This reaction is sometimes called “CO2 insertion” and it increases the number of carbons in the molecule by one.
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19. Hydrolysis of Nitriles
Basic or acidic hydrolysis of a nitrile (—CN) produces a carboxylic acid.
The overall reaction, starting from the alkyl halide, adds an extra carbon to the molecule.
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20. Nucleophilic Acyl Substitution
Carboxylic acids react by nucleophilic acyl substitution, where one nucleophile replaces another on the acyl (C═O) carbon atom.
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21. Fischer Esterification
Reaction of a carboxylic acid with an alcohol under acidic conditions produces an ester.
Reaction is an equilibrium, the yield of ester is not high.
To drive the equilibrium to the formations of products use a large excess of alcohol.
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22. Fischer Esterification Mechanism
Step 1:
The carbonyl oxygen is protonated to activate the carbon toward nucleophilic attack.
The alcohol attacks the carbonyl carbon.
Deprotonation of the intermediate produces the ester hydrate.
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23. Fischer Esterification Mechanism
Step 2:
Protonation of one of the hydroxide creates a good leaving group.
Water leaves.
Deprotonation of the intermediate produces the ester.
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24. Solved Problem 1 Solution
Ethyl orthoformate hydrolyzes easily in dilute acid to give formic acid and three equivalents of ethanol. Propose a mechanism for the hydrolysis of ethyl orthoformate.
Solution
Ethyl orthoformate resembles an acetal with an extra alkoxy group, so this mechanism should resemble the hydrolysis of an acetal (Section 18-18). There are three equivalent basic sites: the three oxygen atoms. Protonation of one of these sites allows ethanol to leave, giving a resonance-stabilized cation. Attack by water gives an intermediate that resembles a hemiacetal with an extra alkoxy group.
Copyright © 2006 Pearson Prentice Hall, Inc.
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25. Solved Problem 1 (Continued)
Solution (Continued)
Protonation and loss of a second ethoxyl group gives an intermediate that is simply a protonated ester.
Copyright © 2006 Pearson Prentice Hall, Inc.
Hydrolysis of ethyl formate follows the reverse path of the Fischer esterification. This part of the mechanism is left to you as an exercise.
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26. Esterification Using Diazomethane
Carboxylic acids are converted to their methyl esters very simply by adding an ether solution of diazomethane.
The reaction usually produces quantitative yields of ester.
Diazomethane is very toxic, explosive. Dissolve in ether.
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27. Mechanism of Diazomethane Esterification
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28. Synthesis of Amides
The initial reaction of a carboxylic acid with an amine gives an ammonium carboxylate salt.
Heating this salt to well above 100° C drives off steam and forms an amide.
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29. LiAlH4 or BH3 Reduction of Carboxylic Acids
LiAlH4 reduces carboxylic acids to primary alcohols.
The intermediate aldehyde reacts faster with the reducing agent than the carboxylic acid.
BH3•THF (or B2H6) can also reduce the carboxylic acid to the alcohol
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30. Reduction of Acid Chlorides to Aldehydes
Lithium aluminum tri(tert-butoxy)hydride is a weaker reducing agent than lithium aluminum hydride.
It reduces acid chlorides because they are strongly activated toward nucleophilic addition of a hydride ion.
Under these conditions, the aldehyde reduces more slowly, and it is easily isolated.
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31. Conversion of Carboxylic Acids to Ketones
A general method of making ketones involves the reaction of a carboxylic acid with two equivalents of an organolithium reagent.
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32. Mechanism of Ketone Formation
The first equivalent of organolithium acts as a base, deprotonating the carboxylic acid.
The second equivalent adds to the carbonyl.
Hydrolysis forms the hydrate of the ketone, which converts to the ketone.
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33. Synthesis of Acid Chlorides
The best reagent for converting carboxylic acids to acid chlorides are thionyl chloride (SOCl2) and oxalyl chloride (COCl2) because they form gaseous by-products that do not contaminate the product.
Thionyl chloride reaction produces SO2 while the oxalyl chloride reaction produces HCl, CO, and CO2 (all gaseous).
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34. Mechanism of Acid Chloride Formation
Step 1
Step 2
Step 3
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35. Esterification of an Acid Chloride
Attack of the alcohol at the electrophilic carbonyl group gives a tetrahedral intermediate. Loss of a chloride and deprotonation gives an ester.
Esterification of an acyl chloride is more efficient than the Fischer esterification.
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36. Amide Synthesis
Ammonia and amines react with acid chlorides to give amides
NaOH, pyridine, or a second equivalent of amine is used to neutralize the HCl produced to prevent protonation of the amine.
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